HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1H-Indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Benzaldehyde, 2-azido-4,5-dimethoxy- | HCID 11344785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1H-Indazole | HCID 9221 | 169.3% |
Reaction Steps
A solution containing 51.8 g (0.25 mole) 6-azidoveratraldehyde (Example XII), 26.0 g (0.28 mole) aniline, 4 ml galcial acetic acid, and 300 ml dimethylformamide was stirred at 90°-100° for 1 hr, then refluxed for 1 hr until the gaseous evolution was complete. After the mixture was cooled and poured slowly in 1.5 1. iced water, the product was filtered, washed with two 150 ml portions cold water, and air dried to give 50 g of crude indazole, m.p. 130°-138°. Recrystallization from ethyl acetate -- hexane followed by ethyl acetate gave 26 g (41%) of the product, m.p. 149°-152°. Recrystallization from ethyl acetate -- hexane gave the analytical sample, m.p. 149°-152° .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014878 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-3a273590390d4abbb975c7648b418a52 |
| Source note | uspto-grants-1977_03 |